Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Saskia Louwrier"'
Publikováno v:
Tetrahedron Letters, 37, 905-908. Elsevier
The synthesis of a tricyclic guanidine as a model compound for ptilomycalin A and related guanidine alkaloids is described. The synthesis starts from succinimide and features an N -acyliminium ion coupling, an Eschenmoser sulfide-contraction and an N
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::26a93f2c2a9032d44f9a800c0986b3e0
https://doi.org/10.1016/0040-4039(95)02258-9
https://doi.org/10.1016/0040-4039(95)02258-9
Publikováno v:
Tetrahedron, 52, 2629-2646. Elsevier
The syntheses of three bicyclic guanidines as model compounds for the guanidine alkaloid ptilomycalin A are described. The guanidines are prepared from pyrrolidin-2-one via an N-acyliminium ion coupling reaction with silyl enol ethers and a direct gu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d3cc9c26ac804a6c5d23e8546f1843ac
https://doi.org/10.1016/0040-4020(95)01086-6
https://doi.org/10.1016/0040-4020(95)01086-6
Publikováno v:
Tetrahedron, 52, 2603-2628. Elsevier
Highly stereoselective N -acyliminium ion coupling reactions of β-ketoester derived silyl enol ethers with enantiopure lactams derived from ( S )-malic acid are reported. This reaction type is applied in the synthesis of the enantiopure C-2 substitu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a2a3b51b8a537e63703eb02bb32e08f1
https://dare.uva.nl/personal/pure/en/publications/studies-towards-the-synthesis-of-ptilomycalin-a-stereoselective-nacyliminium-ion-coupling-reactions-to-enantiopure-c2-substituted-lactams(fa02714d-4917-4308-9b03-211e539c3e13).html
https://dare.uva.nl/personal/pure/en/publications/studies-towards-the-synthesis-of-ptilomycalin-a-stereoselective-nacyliminium-ion-coupling-reactions-to-enantiopure-c2-substituted-lactams(fa02714d-4917-4308-9b03-211e539c3e13).html
Autor:
Henk Hiemstra, M. J. Moolenaar, Saskia Louwrier, R. Van Ginkel, W.‐J. Koot, Mirko Kranenburg, W. N. Speckamp
Publikováno v:
ChemInform. 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e16d3fd7cb89c4dcc5819f77c550cfcc
https://doi.org/10.1002/chin.199149257
https://doi.org/10.1002/chin.199149257
Publikováno v:
ChemInform. 27
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7a31ada99a51db29963a09f017d3df4f
https://doi.org/10.1002/chin.199625105
https://doi.org/10.1002/chin.199625105
Publikováno v:
ChemInform. 27
The syntheses of three bicyclic guanidines as model compounds for the guanidine alkaloid ptilomycalin A are described. The guanidines are prepared from pyrrolidin-2-one via an N-acyliminium ion coupling reaction with silyl enol ethers and a direct gu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5017800e25e8a1d75cb081ec2550b10b
https://doi.org/10.1002/chin.199624159
https://doi.org/10.1002/chin.199624159
Publikováno v:
ChemInform. 27
The synthesis of a tricyclic guanidine as a model compound for ptilomycalin A and related guanidine alkaloids is described. The synthesis starts from succinimide and features an N -acyliminium ion coupling, an Eschenmoser sulfide-contraction and an N
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5e103373de037fb2ff01357bbcedf5bb
https://doi.org/10.1002/chin.199621171
https://doi.org/10.1002/chin.199621171
Autor:
Mirko Kranenburg, Henk Hiemstra, Saskia Louwrier, Roel van Ginkel, M. J. Moolenaar, W.‐J. Koot, W. Nico Speckamp
Publikováno v:
Tetrahedron Letters. 32:401-404
Highly stereoselective syntheses of enantiomerically pure γ-amino acids statine and 4- epi -statine from ( S )-malic acid are described by using, respectively, an intramolecular α-acylamino radical reaction and an intermolecular N -acyliminium ally
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ee215fcec445ce827741131cc8df5eea
https://doi.org/10.1016/s0040-4039(00)92639-x
https://doi.org/10.1016/s0040-4039(00)92639-x